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1000 Titel
  • Diabetic pregnancy as a novel risk factor for cardiac dysfunction in the offspring—the heart as a target for fetal programming in rats
1000 Autor/in
  1. Schütte, Till |
  2. Kedziora, Sarah |
  3. Haase, Nadine |
  4. Herse, Florian |
  5. Alenina, Natalia |
  6. Muller, Dominik N |
  7. Bader, Michael |
  8. Schupp, Michael |
  9. Dechend, Ralf |
  10. Golic, Michaela |
  11. Kräker, Kristin |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-09-18
1000 Erschienen in
1000 Quellenangabe
  • 64(12):2829-2842
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00125-021-05566-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563640/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Aims/hypothesis!#!The impact of diabetic pregnancy has been investigated extensively regarding offspring metabolism; however, little is known about the influence on the heart. We aimed to characterise the effects of a diabetic pregnancy on male adult offspring cardiac health after feeding a high-fat diet in an established transgenic rat model.!##!Methods!#!We applied our rat model for maternal type 2 diabetes characterised by maternal insulin resistance with hyperglycaemia and hyperinsulinaemia. Diabetes was induced preconceptionally via doxycycline-induced knock down of the insulin receptor in transgenic rats. Male wild-type offspring of diabetic and normoglycaemic pregnancies were raised by foster mothers, followed up into adulthood and subgroups were challenged by a high-fat diet. Cardiac phenotype was assessed by innovative speckle tracking echocardiography, circulating factors, immunohistochemistry and gene expression in the heart.!##!Results!#!When feeding normal chow, we did not observe differences in cardiac function, gene expression and plasma brain natriuretic peptide between adult diabetic or normoglycaemic offspring. Interestingly, when being fed a high-fat diet, adult offspring of diabetic pregnancy demonstrated decreased global longitudinal (-14.82 ± 0.59 vs -16.60 ± 0.48%) and circumferential strain (-23.40 ± 0.57 vs -26.74 ± 0.34%), increased relative wall thickness (0.53 ± 0.06 vs 0.37 ± 0.02), altered cardiac gene expression, enlarged cardiomyocytes (106.60 ± 4.14 vs 87.94 ± 1.67 μm), an accumulation of immune cells in the heart (10.27 ± 0.30 vs 6.48 ± 0.48 per fov) and higher plasma brain natriuretic peptide levels (0.50 ± 0.12 vs 0.12 ± 0.03 ng/ml) compared with normoglycaemic offspring on a high-fat diet. Blood pressure, urinary albumin, blood glucose and body weight were unaltered between groups on a high-fat diet.!##!Conclusions/interpretation!#!Diabetic pregnancy in rats induces cardiac dysfunction, left ventricular hypertrophy and altered proinflammatory status in adult offspring only after a high-fat diet. A diabetic pregnancy itself was not sufficient to impair myocardial function and gene expression in male offspring later in life. This suggests that a postnatal high-fat diet is important for the development of cardiac dysfunction in rat offspring after diabetic pregnancy. Our data provide evidence that a diabetic pregnancy is a novel cardiac risk factor that becomes relevant when other challenges, such as a high-fat diet, are present.
1000 Sacherschließung
lokal Fetal Development [MeSH]
lokal Rats, Sprague-Dawley [MeSH]
lokal Risk Factors [MeSH]
lokal Echocardiography
lokal Maternal inheritance
lokal Heart Diseases [MeSH]
lokal Male [MeSH]
lokal Diabetes Mellitus, Type 2/genetics [MeSH]
lokal Rats
lokal Cardiovascular diseases
lokal Diet, High-Fat/adverse effects [MeSH]
lokal Female [MeSH]
lokal Myocytes, Cardiac [MeSH]
lokal Pregnancy
lokal Diabetes mellitus
lokal Rats [MeSH]
lokal Prenatal Exposure Delayed Effects [MeSH]
lokal Animals [MeSH]
lokal Diet
lokal Infant
lokal High-fat
lokal Article
lokal Transgenic
lokal Hyperglycaemia
lokal Pregnancy [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-4869-2766|https://orcid.org/0000-0003-0124-2557|https://orcid.org/0000-0003-0727-1738|https://orcid.org/0000-0002-9305-8134|https://orcid.org/0000-0002-6071-5433|https://orcid.org/0000-0003-3650-5644|https://orcid.org/0000-0003-4780-4164|https://orcid.org/0000-0003-3720-1052|https://orcid.org/0000-0001-6636-3080|https://orcid.org/0000-0003-3030-2678|https://orcid.org/0000-0002-4032-5382
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